Canonical Allele Identifier: CA1931514584
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2039011179
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845994_99845998dup , CM000672.2:g.99845994_99845998dup GRCh38
NC_000010.10:g.101605751_101605755dup , CM000672.1:g.101605751_101605755dup GRCh37
NC_000010.9:g.101595741_101595745dup NCBI36
NG_011798.1:g.68289_68293dup
NG_011798.2:g.68397_68401dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+212_4146+216dup MANE Select ENSP00000497274.1:n.4146+212_4146+216dup
ENST00000648523.1:c.34+212_34+216dup
ENST00000649459.1:n.494+212_494+216dup
ENST00000370449.8:c.4146+212_4146+216dup ENSP00000359478.4:n.4146+212_4146+216dup
NM_000392.4:c.4146+212_4146+216dup NP_000383.1:n.4146+212_4146+216dup
XM_006717630.2:c.3450+212_3450+216dup XP_006717693.1:n.3450+212_3450+216dup
XR_945604.1:n.4276+212_4276+216dup
XR_945605.1:n.4210+212_4210+216dup
NM_000392.5:c.4146+212_4146+216dup MANE Select NP_000383.2:n.4146+212_4146+216dup
XM_006717630.3:c.3450+212_3450+216dup XP_006717693.1:n.3450+212_3450+216dup
XR_945604.3:n.4330+212_4330+216dup
XR_945605.3:n.4262+212_4262+216dup
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